Submission Details
| 510(k) Number | K252467 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 06, 2025 |
| Decision Date | October 27, 2025 |
| Days to Decision | 82 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Statement |
K252467 is an FDA 510(k) clearance for the Disposable Vinyl Examination Gloves, a Vinyl Patient Examination Glove (Class I — General Controls, product code LYZ), submitted by Viet Phu Trade and Import Export Co., Ltd. (Dong Trieu, VN). The FDA issued a Cleared decision on October 27, 2025, 82 days after receiving the submission on August 6, 2025. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.6250.
| 510(k) Number | K252467 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 06, 2025 |
| Decision Date | October 27, 2025 |
| Days to Decision | 82 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Statement |
| Product Code | LYZ — Vinyl Patient Examination Glove |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 880.6250 |
| Definition | A Vinyl Patient Examination Glove Is A Disposable Device Made Of Poly(vinyl Chloride) That May Or May Not Bear A Trace Amount Of Residual Powder, And Is Intended To Be Worn On The Hand For Medical Purposes To Provide A Barrier Against Potentially Infectious Materials And Other Contaminants. |